Yentreve

Medicinal product

(Invented) name

Yentreve

Active substance (s)

Duloksetinas

Strength

20 mg

Pharmaceutical form

skrandyje neirios kietosios kapsulės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

N06AX21, Duloxetine

Marketing authorisation holder

Eli Lilly Nederland B.V., Nyderlandai

Date of authorisation

2004-08-11

Date of renewal

Documents

Search in EMA Europe

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Gastro-resistant capsule, hard	1 vnt.
Duloksetinas	20 mg

Packages

PAKID	NPAKID	NPAKID-7	Pack type	Pack size	Type of packaging	Proposed dispensing/classification	Marketing authorisation no.	Supply status	From	To	Package is in foreign language	From	To	Mock-up
27021	29585	1029585	lizdinė plokštelė	N56		Receptinis	EU/1/04/280/001	Netiekiama	-	-	No	-	-
27022	29586	1029586	lizdinė plokštelė	N28		Receptinis	EU/1/04/280/007	Netiekiama	-	-	No	-	-
27023	29587	1029587	lizdinė plokštelė	N98		Receptinis	EU/1/04/280/008	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2004-08-11	Registruotas